rs121918363, SRPX2

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked
CUI: C1845070
Disease: Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked
3 0.925 0.200 X 100667292 missense variant A/G snv 5.7E-04 4.1E-04 0.700 1.000 1 2006 2006
Epilepsy
CUI: C0014544
Disease: Epilepsy
339 0.925 0.200 X 100667292 missense variant A/G snv 5.7E-04 4.1E-04 0.010 1.000 1 2019 2019